{"uid":"cap_xIVUmYghfYIfUgV_jBf8B","slug":"toolcall-click-medical-device-intelligence-743915e7","name":"toolcall.click Medical Device Intelligence","description":"Keyless pay-per-call APIs for AI agents: 30 tools across compliance, trade, safety, web and data. Pay per call with USDC on Base via x402. No account, no API key.","url":"https://toolcall.click/t/med/device","method":"GET","headers":{},"bodySchema":null,"responseSchema":{"type":"json","example":{"recalls":[],"classification":[{"class":"2","deviceName":"Pump, Infusion, Insulin","regulation":"880.5725"}],"clearances510k":[{"kNumber":"K123456","applicant":"Example Medical","decisionDate":"2024-05-01"}],"adverseEventReports":51234}},"example":null,"exampleRequest":null,"tags":["x402"],"displayCostAmount":"0.02","displayCostAsset":"USDC","priceDynamic":false,"priceHint":null,"priceStatus":"priced","priceSource":"probe","requiresHandshake":false,"reviewCount":0,"rating":{"score":"0.00","successRate":"0.00","reviews":0,"stars":null,"state":"unrated"},"availabilityStatus":"down","priceObserved":null,"sessionDeposit":null,"pricing":{"kind":"static","summary":"$0.04/call","primary":{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.04","per":"call","confidence":"exact"},"accepted":[{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.04","per":"call","confidence":"exact"}]},"paymentMethods":[{"uid":"pm_anSZ26FBluxZ53YcfVG9A","protocol":"x402","methodType":"crypto","chain":"base","mode":"charge","costAmount":"0.04","costPer":"request","priority":0,"asset":"0x833589fCD6eDb6E08f4c7C32D4f71b54bdA02913","unit":"request","depositMicros":null,"planRef":null}],"brandName":null,"brandSlug":null,"brandBaseUrl":null,"brandDocsUrl":null,"whatItDoes":"Aggregates FDA intelligence on any medical device — GUDID identity, device class, 510(k)/PMA status, recalls, and MAUDE adverse-event counts — from openFDA in a single call","exampleAgentPrompt":"Pull up the full FDA regulatory profile for the Abbott FreeStyle Libre — I need the device class, whether it has 510(k) clearance or PMA approval, any recent recalls, and how many adverse events are on file in MAUDE.","exampleUseCases":null,"resultDescription":"A JSON object containing aggregated FDA data for the queried device: GUDID identity fields (product name, manufacturer, UDI), device classification and regulation number, list of 510(k) clearances and/or PMA approvals, recent recall records, and a count of MAUDE adverse-event reports — all sourced live from openFDA in one response.","failureModes":["Device not found in openFDA — returns empty or null results if name/UDI doesn't match any record","Ambiguous device name matches multiple products — may return data for wrong device; use UDI for precision","openFDA API upstream outage — may return 502/503 or timeout","Invalid UDI format — returns error if DI is malformed","Rate limiting or payment failure — call not processed if x402 payment is rejected"],"whenToPreferThis":"Use this endpoint when you need a single-call FDA regulatory summary for a medical device, combining identity, classification, clearance/approval history, recall status, and adverse events from openFDA without having to query multiple FDA databases separately. Prefer over direct openFDA queries when you want aggregated intelligence in one response. Best for regulatory due diligence, device safety checks, competitive research, or compliance workflows.","instructions":null,"reviewSummary":null,"reviewSummaryHighlights":null,"reviewSummaryConcerns":null,"reviewSummaryGeneratedAt":null,"activationCount":0,"lastUsedAt":null,"lastSuccessfullyRanAt":null,"lastHealthCheckAt":"2026-09-15T14:26:09.130Z","isFirstParty":false}